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停乳链球菌 C 群血清型 167 号菌株的全基因组序列及其与停乳链球菌 C 群血清型菌株的比较基因组学分析

Complete genome sequence of Streptococcus dysgalactiae subsp. equisimilis 167 carrying Lancefield group C antigen and comparative genomics of S. dysgalactiae subsp. equisimilis strains.

出版信息

Genome Biol Evol. 2013;5(9):1644-51. doi: 10.1093/gbe/evt117.

Abstract

Streptococcus dysgalactiae subsp. equisimilis (SDSE) is an emerging human pathogen that causes life-threatening invasive infections such as streptococcal toxic shock syndrome. Recent epidemiological studies reveal that invasive SDSE infections have been increasing in Asia, Europe, and the United States. Almost all SDSE carry Lancefield group G or C antigen. We have determined the complete genome sequence of a human group C SDSE 167 strain. A comparison of its sequence with that of four SDSE strains, three in Lancefield group G and one in Lancefield group A, showed approximately 90% coverage. Most regions showing little or no homology were located in the prophages. There was no evidence of massive rearrangement in the genome of SDSE 167. Bayesian phylogeny using entire genome sequences showed that the most recent common ancestor of the five SDSE strains appeared 446 years ago. Interestingly, we found that SDSE 167 harbors sugar metabolizing enzymes in a unique region and streptodornase in the phage region, which presumably contribute to the degradation of host tissues and the prompted covRS mutation, respectively. A comparison of these five SDSE strains, which differ in Lancefield group antigens, revealed a gene cluster presumably responsible for the synthesis of the antigenic determinant. These results may provide the basis for molecular epidemiological research of SDSE.

摘要

无乳链球菌(Streptococcus dysgalactiae subsp. equisimilis,SDSE)是一种新兴的人类病原体,可引起危及生命的侵袭性感染,如链球菌中毒性休克综合征。最近的流行病学研究表明,侵袭性 SDSE 感染在亚洲、欧洲和美国呈上升趋势。几乎所有的 SDSE 都携带 Lancefield 组 G 或 C 抗原。我们已经确定了人类 C 组 SDSE 167 株的完整基因组序列。将其序列与其他 4 株 SDSE 序列(3 株属于 Lancefield 组 G,1 株属于 Lancefield 组 A)进行比较,发现大约有 90%的序列是同源的。显示很少或没有同源性的大多数区域都位于噬菌体中。SDSE 167 基因组中没有明显的大规模重排证据。使用全基因组序列进行的贝叶斯系统发育分析表明,这 5 株 SDSE 的最近共同祖先出现在 446 年前。有趣的是,我们发现 SDSE 167 在一个独特的区域中含有糖代谢酶,在噬菌体区域中含有链道酶,这可能分别有助于宿主组织的降解和 covRS 突变的发生。对这 5 株 Lancefield 组抗原不同的 SDSE 菌株进行比较,揭示了一个可能负责合成抗原决定簇的基因簇。这些结果可能为 SDSE 的分子流行病学研究提供基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebf/3787669/31442ec8526f/evt117f1p.jpg

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